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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864304Generated: November 1, 2026

3-Fluorobenzyl chloride → HCID 57974306, compound

https://huagongshe.com/reaction/1864304

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluorobenzyl chlorideHCID 9974—
ReactantHCID 69056760HCID 69056760—
ProductHCID 57974306HCID 5797430625%

Reaction Steps

The procedure described in Example 3 was repeated using 1-(chloromethyl)-3-fluorobenzene and 2-hydroxy-N-[(2R)-2-({4-[(4-hydroxy-3-methylphenyl)amino]quinazolin-5-yl}oxy)propyl]acetamide (obtained as described in Example 82, preparation of starting materials) to give the title compound as a light yellow solid in 25% yield; NMR spectrum (DMSO-d6) 1.39 (d, 3H), 2.25 (s, 3H), 3.42 (dt, 1H), 3.72 (dt, 1H), 3.81 (d, 2H), 4.94 (m, 1H), 5.17 (s, 2H), 5.47 (t, 1H), 6.99 (d, 1H), 7.16 (td, 1H), 7.22 (d, 1H), 7.30 (m, 3H), 7.43 (m, 1H), 7.56 (d, 1H), 7.61 (dd, 1H), 7.68 (t, 1H), 8.16 (t, 1H), 8.43 (s, 1H), 9.94 (s, 1H); Mass spectrum MH+ 491.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625908B2
Source datasetuspto-grants-2009_12
ORD IDord-43942c28edb34d67af35e2b91681032a
Source noteuspto-grants-2009_12